Formation of manganese oxides by bacterially generated superoxide

Nature Geoscience

Volumn 4, Issue 2, 2011, Pages 95-98

  Learman, D R ^a   Voelker, B M ^b   Vazquez Rodriguez, A I ^a   Hansel, C M ^a  

^a HARVARD UNIVERSITY   (United States)

^b Department of Geology and Geological Engineering   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANOXIC CONDITIONS; BIOMINERALIZATION; CARBON; DEGRADATION; ENZYME ACTIVITY; MANGANESE OXIDE; METABOLISM; MICROBIAL ACTIVITY; NUTRIENT CYCLING; OXIDATION;

BACTERIA (MICROORGANISMS); ROSEOBACTER; ROSEOBACTER SP. AZWK-3B;

EID: 79551599746     PISSN: 17520894     EISSN: 17520908     Source Type: Journal    
DOI: 10.1038/ngeo1055     Document Type: Article

References (29)

1. Nealson, K. H., Tebo, B. M. & Rosson, R. A. Occurrence and mechanisms of microbial oxidation of manganese. Adv. Appl. Microbiol. 33, 279-318 (1988).
2. Tebo, B. M., Johnson, H. A., McCarthy, J. K. & Templeton, A. S. Geomicrobiology of manganese(ii) oxidation. Trends Microbiol. 13, 421-428 (2005).
3. Tebo, B. M., Ghiorse, W. C., vanWaasbergen, L. G., Siering, P. L. & Caspi, R. Reviews in Mineralogy Vol. 35, 225-266 (The Mineralogical Society of America, 1997).
4. 2 in absence of Mn-bacteria or surface catalysts. Geochim. Et Cosmochim. Acta 48, 1571-1573 (1984).
5. Davies, S. H. R. & Morgan, J. J. Manganese(ii) oxidation-kinetics on metal-oxide surfaces. J. Colloid Interface Sci. 129, 63-77 (1989).
6. Gonzalez, J. M. & Moran, M. A. Numerical dominance of a group of marine bacteria in the alpha-subclass of the class Proteobacteria in coastal seawater. Appl. Environ. Microbiol. 63, 4237-4242 (1997).
7. Templeton, A. S., Staudigel, H. & Tebo, B. M. Diverse Mn(ii)-oxidizing bacteria isolated from submarine basalts at Loihi Seamount. Geomicrobiol. J. 22, 127-139 (2005).
8. Buchan, A., Gonzalez, J. M.&Moran, M. A. Overview of the marine Roseobacter lineage. Appl. Environ. Microbiol. 71, 5665-5677 (2005).
9. Godrant, A., Rose, A. L., Sarthou, G. & Waite, T. D. New method for the determination of extracellular production of superoxide by marine phytoplankton using the chemiluminescence probes MCLA and red-CLA. Limnol. Oceanogr.-Meth. 7, 682-692 (2009).
10. Archibald, F. S. & Fridovich, I. The scavenging of superoxide radical by manganous complexes: In vitro. Arch. Biochem. Biophys. 214, 452-463 (1982).
11. Barnese, K., Gralla, E. B., Cabelli, D. E. & Valentine, J. S. Manganous phosphate acts as a superoxide dismutase. J. Am. Chem. Soc. 130, 4604 (2008).
12. Hansel, C. M. & Francis, C. A. Coupled photochemical and enzymatic Mn(ii) oxidation pathways of a planktonic Roseobacter-like bacterium. Appl. Environ. Microbiol. 72, 3543-3549 (2006).
13. Webb, S. M., Dick, G. J., Bargar, J. R. & Tebo, B. M. Evidence for the presence of Mn(iii) intermediates in the bacterial oxidation of Mn(ii). Proc. Natl Acad. Sci. USA 102, 5558-5563 (2005).
14. Brouwers, G. J. et al. Stimulation of Mn(ii) oxidation in Leptothrix discophora SS-1 by Cu2C and sequence analysis of the region flanking the gene encoding putative multicopper oxidase MofA. Geomicrobiol. J. 17, 25-33 (2000).
15. -) in seawater: Reactions with inorganic copper complexes. J. Phys. Chem. A 102, 5693-5700 (1998).
16. Voelker, B. M., Sedlak, D. L. & Zafiriou, O. C. Chemistry of superoxide radical in seawater: Reactions with organic Cu complexes. Environ. Sci. Technol. 34, 1036-1042 (2000).
17. Gonzalez-Gil, G., Jansen, S., Zandvoort, M. H. & van Leeuwen, H. P. Effect of yeast extract on speciation and bioavailability of nickel and cobalt in anaerobic bioreactors. Biotechnol. Bioeng. 82, 134-142 (2003).
18. Bedard, K., Lardy, B. & Krause, K. H. NOX family NADPH oxidases: Not just in mammals. Biochimie 89, 1107-1112 (2007).
19. Huycke, M. M. et al. Extracellular superoxide production by Enterococcus faecalis requires demethylmenaquinone and is attenuated by functional terminal quinol oxidases. Mol. Microbiol. 42, 729-740 (2001).
20. Lin, P. C., Turk, K., Hase, C. C., Fritz, G. & Steuber, J. Quinone reduction by the NaC-translocating NADH dehydrogenase promotes extracellular superoxide production in Vibrio cholerae. J. Bacteriol. 189, 3902-3908 (2007).
21. Korshunov, S. & Imlay, J. A. Detection and quantification of superoxide formed within the periplasm of Escherichia coli. J. Bacteriol. 188, 6326-6334 (2006).
22. Johnson, H. A. & Tebo, B. M. In vitro studies indicate a quinone is involved in bacterial Mn(ii) oxidation. Arch. Microbiol. 189, 59-69 (2008).
23. El Gheriany, I. A. et al. Iron requirement for Mn(ii) oxidation by Leptothrix discophora SS-1. Appl. Environment. Microbiol. 75, 1229-1235 (2009).
24. Sunda, W. G. & Huntsman, S. A. Photoreduction of manganese oxides in seawater. Mar. Chem. 46, 133-152 (1994).
25. Voelker, B. M. & Sedlak, D. L. Iron reduction by photoproduced superoxide in seawater. Mar. Chem. 50, 93-102 (1995).
26. Vermilyea, A. W., Hansard, S. P.&Voelker, B. M. Dark production of hydrogen peroxide in the Gulf of Alaska. Limnol. Oceanogr. 55, 580-588 (2010).
27. Rose, A. L., Webb, E. A., Waite, T. D. & Moffett, J. W. Measurement and implications of nonphotochemically generated superoxide in the equatorial Pacific Ocean. Environ. Sci. Technol. 42, 2387-2393 (2008).
28. Kustka, A. B., Shaked, Y., Milligan, A. J., King, D. W. & Morel, F. M. M. Extracellular production of superoxide by marine diatoms: Contrasting effects on iron redox chemistry and bioavailability. Limnol. Oceanogr. 50, 1172-1180 (2005).
29. Goldstein, S., Fridovich, I. & Czapski, G. Kinetic properties of Cu, Zn-superoxide dismutase as a function of metal content-order restored. Free Radical Biol. Med. 41, 937-941 (2006).